1. A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneity. (26th January 2021) Authors: Butbul Aviel, Yonatan; Ofir, Ayala; Ben-Izhak, Ofer; Vlodavsky, Euvgeni; Karbian, Netanel; Brik, Riva; Mevorach, Dror; Magen, Daniella Journal: Rheumatology Issue: Volume 60:Number 10(2021) Page Start: 4888 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Demyelination, strokes, and eculizumab: Lessons from the congenital CD59 gene mutations. (September 2017) Authors: Tabib, Adi; Karbian, Netanel; Mevorach, Dror Journal: Molecular immunology Issue: Volume 89(2017:Sep.) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Eculizumab Is Safe and Effective as a Long-term Treatment for Protein-losing Enteropathy Due to CD55 Deficiency. Issue 3 (March 2019) Authors: Kurolap, Alina; Eshach Adiv, Orly; Hershkovitz, Tova; Tabib, Adi; Karbian, Netanel; Paperna, Tamar; Mory, Adi; Vachyan, Arcadi; Slijper, Nadav; Steinberg, Ran; Zohar, Yaniv; Mevorach, Dror; Baris Feldman, Hagit Journal: Journal of pediatric gastroenterology and nutrition Issue: Volume 68:Issue 3(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Prothrombotic mechanisms in patients with congenital p.Cys89Tyr mutation in CD59. Issue 168 (August 2018) Authors: Tabib, Adi; Hindi, Issam; Karbian, Netanel; Zelig, Orly; Falach, Batla; Mevorach, Dror Journal: Thrombosis research Issue: Issue 168(2018) Page Start: 67 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Successful eculizumab therapy for clinical syndromes caused by CD59 and CD55 deficiencies. (October 2018) Authors: Karbian, Netanel; Kurolap, Alina; Eshach-Adiv, Orly; Tabib, Adi; Baris, Hagit; Mevorach, Dror Journal: Molecular immunology Issue: Volume 102(2018:Oct.) Page Start: 188 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Therapy with eculizumab for patients with primary p.Cys89Tyr mutation in the CD59 gene avoids recurrent arterial thrombosis. (September 2017) Authors: Mevorach, Dror; Tabib, Adi; Karbian, Netanel Journal: Molecular immunology Issue: Volume 89(2017:Sep.) Page Start: 186 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗